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Congenital Rhabdomyosarcoma: a different clinical presentation in two cases
BACKGROUND: Rhabdomyosarcoma (RMS), one of the most common soft tissue sarcomas of childhood, is very rare in the neonatal period (0.4–2% of cases). In order to gain a deeper understanding of this disease at such age, patient and tumor features, as well as treatment modality and outcome need to be r...
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| Publicat a: | BMC Pediatr |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5953406/ https://ncbi.nlm.nih.gov/pubmed/29764408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-018-1128-5 |
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